Skip to content
Sinfony

Pharmaceutical industry

Your GMP compliance rests on critical actions. Secure them.

In pharmaceutical production, GMP compliance plays out at the workstation: on an intervention in a sterile area, a weighing, a batch-record review, a deviation handling. This critical know-how stays largely informal, in the heads of your experienced operators, your QA and your QC. Sinfony captures it so that mastery — and data integrity — no longer depend on key people.

Sterile pharmaceutical production environment illustrated in a modern, clean style

The problem

Validated doesn't mean mastered.

Your SOPs are approved, your training records signed off. But between the procedure and the real action in sterile production, the gap remains — and it fuels deviations, recurring CAPAs and inspection observations. Data integrity, asepsis and batch release demand a consistent execution that documentation alone cannot guarantee.

100%

of staff must be trained for their activities: a GMP requirement, not an option.

Source: 21 CFR 211.25 (eCFR)

80%

of critical know-how stays informal, held by a few operators and QA/QC experts.

Sinfony field observation

Deviations & CAPA

Cut recurring deviations by tackling the root cause: the poorly transmitted action.

Data integrity

Embed the right ALCOA+ reflexes into daily practice at the workstation.

Sterile production

Secure aseptic interventions through the filmed, standardized action.

Our results

The proof, in numbers.

What pharmaceutical sites see once their critical actions are captured.

−15 to −30%
deviations
−50%
deviation handling time
−95%
training-related errors
20,000
certificates that stand up to inspectors
"You're the consultants with the nerve to actually make things move."
Novo Nordisk

Request an assessment.

A Sinfony expert reviews your deviations, your SOPs and your critical GMP actions with your teams.